US2921006A - Polymerization with high energy electrons - Google Patents
Polymerization with high energy electrons Download PDFInfo
- Publication number
- US2921006A US2921006A US291541A US29154152A US2921006A US 2921006 A US2921006 A US 2921006A US 291541 A US291541 A US 291541A US 29154152 A US29154152 A US 29154152A US 2921006 A US2921006 A US 2921006A
- Authority
- US
- United States
- Prior art keywords
- polymerization
- monomer
- electrons
- high energy
- dose
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000006116 polymerization reaction Methods 0.000 title description 54
- 239000000203 mixture Substances 0.000 claims description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 20
- 238000009825 accumulation Methods 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 9
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 8
- 150000005846 sugar alcohols Polymers 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 230000001678 irradiating effect Effects 0.000 claims description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 54
- 229920000180 alkyd Polymers 0.000 description 18
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000005855 radiation Effects 0.000 description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000004641 Diallyl-phthalate Substances 0.000 description 6
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 125000005395 methacrylic acid group Chemical class 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- PVLVQTYSRICFCB-ODZAUARKSA-N (z)-but-2-enedioic acid;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.OC(=O)\C=C/C(O)=O PVLVQTYSRICFCB-ODZAUARKSA-N 0.000 description 3
- GIMMHOVXBFGWHN-UHFFFAOYSA-N C(CCCCC(=O)O)(=O)O.C(C=C/C(=O)O)(=O)O.C(COCCO)O Chemical compound C(CCCCC(=O)O)(=O)O.C(C=C/C(=O)O)(=O)O.C(COCCO)O GIMMHOVXBFGWHN-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- -1 vinyl compounds Chemical class 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
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- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
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- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
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- 229910000679 solder Inorganic materials 0.000 description 2
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- 210000001364 upper extremity Anatomy 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- HIEXFSLRRICUMF-JITBQSAISA-N (e)-but-2-enedioic acid;phthalic acid;propane-1,2-diol Chemical compound CC(O)CO.OC(=O)\C=C\C(O)=O.OC(=O)C1=CC=CC=C1C(O)=O HIEXFSLRRICUMF-JITBQSAISA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- JFZBUNLOTDDXNY-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)propoxy]propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)OCC(C)OC(=O)C(C)=C JFZBUNLOTDDXNY-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- WNGDGLDJIWDQAB-UHFFFAOYSA-N 5-(2-methylprop-2-enoyloxy)pentyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCOC(=O)C(C)=C WNGDGLDJIWDQAB-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 241001364889 Helius Species 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 235000001484 Trigonella foenum graecum Nutrition 0.000 description 1
- 244000250129 Trigonella foenum graecum Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
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- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000254 damaging effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
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- 210000003414 extremity Anatomy 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229920005570 flexible polymer Polymers 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013526 supercooled liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 108010027345 wheylin-1 peptide Proteins 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J33/00—Discharge tubes with provision for emergence of electrons or ions from the vessel; Lenard tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B13/00—Conditioning or physical treatment of the material to be shaped
- B29B13/08—Conditioning or physical treatment of the material to be shaped by using wave energy or particle radiation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21K—TECHNIQUES FOR HANDLING PARTICLES OR IONISING RADIATION NOT OTHERWISE PROVIDED FOR; IRRADIATION DEVICES; GAMMA RAY OR X-RAY MICROSCOPES
- G21K5/00—Irradiation devices
- G21K5/10—Irradiation devices with provision for relative movement of beam source and object to be irradiated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0866—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using particle radiation
- B29C2035/0877—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using particle radiation using electron radiation, e.g. beta-rays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2055/00—Use of specific polymers obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in a single one of main groups B29K2023/00 - B29K2049/00, e.g. having a vinyl group, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
- B29K2067/06—Unsaturated polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0002—Condition, form or state of moulded material or of the material to be shaped monomers or prepolymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0085—Copolymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/18—Grafting textile fibers
Definitions
- agents introduces undesirable by-products in the finally polymerized compositions, which are often difiicult to remove and may deleteriously affect the properties ,of the polymerized materials.
- heat alone for polymerization purposes is slow and often results in.deleterious decomposition.
- Polymerization by light irradiation generally gives poor yields and is applicable to few polymerizable compounds.
- This invention relates to polymerization of polymerizable organic compounds with high energy electrons and, more particularly, to polymerization of such compounds in the liquid or solid state by irradiation with high energy electrons.
- Fig. l is a partially sectionalized, simplified view of accelerator apparatus useful in practicing the invention
- Figs. 2 and 3 are graphs utilized for explaining features of the invention
- Fig. 4 is a partially sectionalized view of alterna- 2,921,006 C P tented Jan. 12, 1960 r 2 invention
- Figs. 7 and 8 illustrate apparatus for obtaining dimensionally specific polymerization in accordance with the invention
- Figs. 9 and 10 are schematic representations of apparatus suitable for continuous polymerization according to the invention.
- High voltage apparatus. 1 capable of producing a beam of high energy electrons for irradiating monomers in accordance with the invention.
- High voltage apparatus l- may be of the type disclosed in United States. Patent No. 2,144,518, patented by Willem F. Westendorp on January 17, 1939, and assigned to the assignee of the present invention.
- this apparatus comprises a resonant system having an open-magnetic circuit inductance coil (not shown) which is positioned within a tank 2 and energized by a source of alternating voltage to generate a'high voltage across its extremities.
- a source of electrons which is maintained at the potential of the upper extremity of the inductance coil whereby a pulseof electrons is accelerated down envelope 3,0nce during eachcycle of the energizing voltage when the upper extremity of the inductance coil is at a negative potential with respect to the lower end.
- an elongated metal tube 4 the upperportion '5 of which is hermetically sealed to tank 2, as illustrated, by any convenient means such assilver solder.
- the lower portion 6 of tube is conical in cross section to permit an increased angular spread of the electron beam.
- amend-window 7 which may be hermetically sealed to tube 4 by means of silver solder.
- Endwindow 7 should be thin enough, to permit electrons of desired energy to pass therethrough but thick enough to withstand the' force of atmospheric pressure.
- Stainless steel of about 0.002 inch thickness has been found satisfactory for use with electron energies of about 230,000 electron volts or .greater.
- end-window 7 in arcuate shape as shown, greater strength for resisting the force of atmospheric pressure may be obtained for a given window thickness. Desiredfocusing of the accelerated electrons may be secured by a magnetic-field generating winding 8 energized by a source of direct current 9' through a variable resistor 9.
- a receptacle 10 containing a liquid monomeer 11 may be supported in the path of the electrons emerging from end-window 7 as illustrated.
- the high energy electrons penetrate the monomer 11 to'a depth dependent upon their energy and initiate'polymerization of the monomer to form solid products of polymer.
- the monomer 11 may comprise monohydric and polyhydric alcohol esters of acrylic and methacrylic acids.
- Monohydric 'alcohols which may be emplyoyed in the preparation of esters of acrylic and methacrylic acids are, for example, methyl, ethyl, propyl, isopropyl, butyl, 2-ethylhexyl, decyl, etc.
- Figs.. 5 and 6 are graphs useful in explaining other features of the preparation of esters of acrylic and methacrylic acids are, for example, ethylene glycol, diethylene glycol, dipropylene glycol, pentamethylene glycol, tetraethylene glycol, glycerine, sorbitol, etc.
- esters prepared from the foregoing alcohols are, for example,
- ethyl acrylate ethyl methacrylate, butyl acrylate, methyl acrylate, methyl methacrylate, dipropylene glycol dimethacrylate, tetraethylene glycol, diacrylate, pentamethylene glycol dimethacrylate, glyccryl trimethacrylate, tetraethylene glycol 'dimethacryl ate, etc.
- Monomer '11 may also comprise acrylom'trile, vinyl chloride, and mixtures of an unsaturated alkyd resin with either styrene or diallyl phthalate.
- Unsaturated alkyd resins employed in the practice of the present invention are those commonly obtained by effecting a reaction between a polyhydric alcohol, many examples of which are stated'above, and an alpha unsaturated alpha, beta dicarboxylic acid or anhydride, whichfor brevity will hereinafter be referred to as unsaturated acid. Examples of such unsaturated acids arevrnaleic acid or anhydride,-fumaric acid. itaconic acid or anhydride, mesaconie acid, etc.
- roentgen unit is the amount of radiation that produces one electrostatic unit of ion pairs per milliliter of dry air under standard cond itions, and as employed here, refers to the amount of electron radiation measured with an air equivalent ionization chamber at the position of the surface of the monomers.
- the percent polymerization for a given total dose administered ,at a given dose accumulation rate is furthermorerdependentupon the initial temperature of the monomer.
- the percent polymerization increases wi h 4 creases in the initial temperature.
- Apparatus for maintaining the monomer undergoing irradiation at a temperature below ambient is illustrated in Fig. 4 wherein numerals employed hereinbefore are utilized to identify like elements.
- Receptacle 10 containing monomer 11 is supported within a cup-shaped member 12 of conducting material such as aluminum by means of a plurality of posts 13 which may consist of wood.
- Member 12 is positioned within a thermally-insulated vacuum bottle 14 upon a pedestal 15 constructed of a material such as a molded product made from a phenol-aldehyde resin.
- a cooling medium 16 such as liquefied nitrogen or air
- tube 17 monomer 11 may be maintained at a desired temperaturebelow ambient, and by slowly adding cooling medium'to compensate for evaporation, the temperature may be controlled. Temperature measurements may be made by any convenient means, e.g., by introducing a thermocouple (not shown) into the center of monomer 11.
- Figs. 7 and 8 whereinlike numerals are use'd to identifyelernents hereinbefore described.
- Figa lreceptacle *10 is shown with a sheet 22 of lead foil positioned over the month thereof.
- Sheet 22 is of sufficient thickness to prevent the passage therethrough of electrons emerging through window 7, but has an opening 23 which'allows a selected portion of the electrons to reach monomer 11.
- Fig. 8 illustrates the solidpolymerproduct 24 having the shape of opening 23, which is produced by irradiation of monomer 11 through opening 23. From an examination of Figs.
- the depth and extent of polymerization, particufollowing example is given by way of illustration and not larly of the crosslinking monomers, may be greatly by way of limitation.
- mice recited in Table I of the following example are Agitation may be accomplished by stirring or by moveall by weight.
- the apparatus used for elfecting the polyment of the receptacle 10 during irradiation. lt may merization described below is that shown in Fig. l and also be'obtained by directing a stream of nitrogen or particularly described above.
- diallyl phthalate alone fails to polymonomeric compositions described in Table I below were merize with high energy electrons but copolymerizesquite polymerized by placing them in receptacle 10 shown in readily in a mixture with an unsaturated alkyd resin Fig. 1.and irradiating them with high energy electrons such as diethylene glycol maleate.
- the weight ratio of at a distance of approximately 10 centimeters using the the diallyl phthalate to the unsaturated alkyd resin may total doses and times recited in the said table.
- the products obtained in accordance with the polymerization process herein described are useful inffor instance, various molding, laminating, and coating ap-v plications.
- the polymers herein disclosed because of the absence of contaminants often present when using vinyl polymerization catalysts, can he expected to have improved electrical properties and'ar'e more resistant to deterioration at high'temperatureQetc.
- Continuous polymerization of the monomers may be obtained with apparatus sucli'as that illustrated in'Figs. 9 and 10 wherein similar numerals are utilized to identify like elements hereinbefore described.
- the monomer in bulk, solution or emulsion is stored in a tank 25 and sprayed through a header 26 upon a moving belt 27.
- Belt 27 may comprise a continuous thin sheet 28 of metal, such as stainless steel about 0.002 inch in thickness, extending around pulleys 29 and 3 0."'To retain the monomer upon belt 27, flanges 31 of a resilient inaterial such as silicone rubber are positioned along the edges of belt 27.
- One of the pulleys 29 311 may be connected to a driven shaft (not shown) so that the monomer, after being sprayed upon belt 27, passes under end-window 7, as is indicated by arrow 32, and is irradiated byhigh energy. electrons. After irradiation and polymerization, the polymer and excess monomer are deposited in a tank 33'Wh e're they are available for utilization. Member 34 serves to scrape the. polymer and monomer from belt 27 and to direct the mixture into tank 33.
- a structure 35 of refractory material may be positioned about belt 27 and the temperature therewithin may be elevated for the purpose of aiding polymerization as above mentioned.
- a window 36 of thin aluminum foil is inserted in the side of structure 35 and in the path of the electron beam so that the energy of the electrons will not be needlessly absorbed.
- Surface inhibitions of the monomer may be prevented by passing a gas such as nitrogen, argon or'heliu m into structure 35 through an inlet'37.
- Roentgen or roentgens have been employed as the units used for measuring'high energy radiation, it will be apparent that one could also employ the term Roentgen equivalent physica or 'REPl interchangeably with the roentgen unit.
- Roentgen units are more commonly used to measure, gamma and X-rays and are usually defined as the amount, of radiation that produces one electrostatic unit or charge per milliliter of dry air under standard conditions.
- the Roentgen equivalent physical unit (the REP) is a convenient unit which usually describes the radiation dose from other than gamma or X -rays, and is the'rneasure of the ionization in'the absorber, or tissue;
- the ionization produced by primary radiation is expressed as one rep when the energy lost in tissue is equivalent to the energy lost by theabsorption ofone Roentgen of gamma or X-rays in air;
- Further :definit'ions of roentgen and REP can be found on page 256 of The Science and Engineering of Nuclear Power, edited by ClarkGoodrnan (1947), and on page 436 of NuclearRadiation Physics, by Lapp and Andrews (1948).
- the process which comprises irradiating with high energy electrons derived from a high voltage accelerating apparatus at a dose accumulation rate ranging from about 0.-0 01 1O to 1x10 REPs per second to a total dose of from 2.5 to 7.5 x10 REPs, a mixture of ingredients comprising, by weight, (1) from 25 to 70% of an unsaturated alkyd resin obtained by the reaction of a polyhydric alcohol and an alpha unsaturated'alpha, beta dicarboxylic acid and (2.) from 30 to of an olefinic material selected from the class consisting of styrene, butyl acrylate, diallyl phathalate, andmixtures of said olefinic materials, the energy of electrons ranging from about 200,000 electronvolts to 20,000,000 electron volts and the said irradiation being continued until a solid polymer is obtained.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Physics & Mathematics (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
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- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE520401D BE520401A (de) | 1952-06-03 | ||
US291541A US2921006A (en) | 1952-06-03 | 1952-06-03 | Polymerization with high energy electrons |
GB15192/53A GB762953A (en) | 1952-06-03 | 1953-06-01 | Improvements in and relating to the polymerization of organic compounds with high energy electrons |
FR1079401D FR1079401A (fr) | 1952-06-03 | 1953-06-02 | Procédé de polymérisation par les électrons de grande énergie |
DEG11888A DE956542C (de) | 1952-06-03 | 1953-06-04 | Verfahren zur Polymerisation von ungesaettigten Alkydharzen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US291541A US2921006A (en) | 1952-06-03 | 1952-06-03 | Polymerization with high energy electrons |
Publications (1)
Publication Number | Publication Date |
---|---|
US2921006A true US2921006A (en) | 1960-01-12 |
Family
ID=23120724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US291541A Expired - Lifetime US2921006A (en) | 1952-06-03 | 1952-06-03 | Polymerization with high energy electrons |
Country Status (5)
Country | Link |
---|---|
US (1) | US2921006A (de) |
BE (1) | BE520401A (de) |
DE (1) | DE956542C (de) |
FR (1) | FR1079401A (de) |
GB (1) | GB762953A (de) |
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US4227980A (en) * | 1978-09-13 | 1980-10-14 | Whittaker Corporation | Photoreactive coating compositions based on urethane modified acrylates |
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US2961388A (en) * | 1956-07-25 | 1960-11-22 | Monsanto Chemicals | Dimerization of trichloroethylene |
US2959531A (en) * | 1956-08-01 | 1960-11-08 | Phillips Petroleum Co | Solid resins from irradiated epoxidized liquid conjugated diene polymers |
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US2967137A (en) * | 1956-11-21 | 1961-01-03 | Gen Electric | Irradiation of nylon |
US3006830A (en) * | 1957-05-31 | 1961-10-31 | Dow Chemical Co | Method for improving the dyeability of fiber-forming cellulose esters |
US2998329A (en) * | 1957-08-05 | 1961-08-29 | Dow Chemical Co | Modification of cellulosic articles |
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US3068122A (en) * | 1958-03-10 | 1962-12-11 | Du Pont | Selected graft polymers and their preparation |
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US3098806A (en) * | 1959-12-10 | 1963-07-23 | Gen Mills Inc | Cross linking of fatty polyamides with ionizing radiation |
US3188229A (en) * | 1961-10-03 | 1965-06-08 | Du Pont | Process of adhering an organic coating to a substrate |
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Cited By (63)
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US3092563A (en) * | 1963-06-04 | Experiment iv | ||
US3372100A (en) * | 1956-02-14 | 1968-03-05 | Raychem Corp | Process for improving the properties of a polymer by cross-linking in the presence of radiation |
US3113087A (en) * | 1957-07-24 | 1963-12-03 | Schlumberger Well Surv Corp | Methods and apparatus for the investigation of materials by radiation |
US3121672A (en) * | 1957-09-04 | 1964-02-18 | Bx Plastics Ltd | Manufacture of new graft copolymers |
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Also Published As
Publication number | Publication date |
---|---|
GB762953A (en) | 1956-12-05 |
FR1079401A (fr) | 1954-11-30 |
BE520401A (de) | |
DE956542C (de) | 1957-01-17 |
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